introduction to organic chemistry Flashcards
(32 cards)
what is the definition of functional group?
the atom or group of atoms that is responsible for most of the chemical reactions of a molecules
what’s the definition of homologous series?
a family of compounds with the same general formula and similar chemical properties
what is the definition of hydrocarbon?
molecules containing hydrogen and carbon only
what’s the definition of stereoisomers?
molecules with the same molecular and structural formulae but a different spatial arrangement of atoms
what is the definition of saturated?
molecules containing no double bonds
what is structural isomer?
molecules with the same molecular formula but different structures
what is chain isomer?
structural isomers that differ by having a different carbon chain
what is position isomer?
structural isomers that differ by having the functional group in a different place
what is functional group isomer?
structural isomers that differ by having a different functional group
what is molecular formula?
formula that gives the actual number of atoms of each element in one molecule
what is the empirical formula
formula that gives the simplest ratio of atoms of each element in a compound
what is the structural formula?
this shows how the atoms are joined together in a molecule
what is the displayed formula?
this shows all the bonds and atoms in a molecule
what is the skeletal formula?
this uses lines to represent bonds. each point represents a c atoms
what are alkanes a homologous series of?
-saturated hydrocarbons with the general formula CnH2n+2.
-this means that they are made of hydrogen and carbon only and contain only carbon-carbon single bonds
what properties will alkanes have since they’re from the same homologous group?
- same functional group
-same general formula
-same chemical properties
-differ in their chemical formula by one CH2 group
-have gradually changing physical properties
how do you name alkanes?
- of their are any side chains/functional groups present then the position of these groups is indicated by numbering the carbon atoms in the longest chain starting at the end that gives the lowest possible numbers in the name
2.the hydrocarbon side chain is shown in brackets in the structural formula
3.the side chain is named by adding “yl” to the normal alkane stem. This type of group is called an alkyl group
4.if there are more than one of the same alkyl side chain or functional groups, di (2), tri (3) or tetra (4) is added in front of its name - the adjacent numbers are separated from words by a hyphen
- if there is more than one type of alkyl side chain, they are listed in alphabetical order
different types of functional group
C=C in alkenes
OH in alcohols
how do you name halogenoalkanes?
1.Name the longest carbon chain in the compound and add the suffix “-ane”.
2.Add a prefix to indicate the halogen atoms:
* Fluoro: For fluorine
* Chloro: For chlorine *Bromo: For bromine
* lodo: For iodine
3. The functional is indicated by a prefix or suffix. e.g. chloroethane
4. The position of the functional group is given by a number, counting from the end that gives the functional group the lowest number
5. Where there are two or more of the same groups, di, tri- or tetra are used.
6. If there is more than one functional group, numbers are separated by commas and the groups are listed in alphabetical order (ignoring di, tri, etc.).
7. If a number is not necessary (i.e. the group could only be in one place) then no number should be given.
8. Numbers are separated by commas and word and numbers by dashes
why is 1-chloropentane and 2-chloropentane position isomers?
they have the same molecular formula but the chlorine atoms is attached to a different carbon atom
what are the 3 different types of halogenoalkane?
positioning of the halogen atoms is used to classify halogenoalkanes
1.primary (1°) halogenoalkane- carbon joined to halogen is attached to one other alkyl group
2.secondary (2°) halogenoalkane- carbon joined to halogen is attached to two other alkyl groups
3.tertiary (3°) halogenoalkane- carbon joined to halogen is attached to three other alkyl groups
what are the properties of alkenes
*Alkenes are unsaturated hydrocarbons with at least one carbon-to-carbon double bond.
* Alkenes are hydrocarbons (i.e. made up of carbon and hydrogen atoms).
* Alkenes are more reactive than alkanes because of the double bond.
* Alkenes can undergo addition reactions, where one molecule combines with another to form a larger molecule. For example, alkenes can react with hydrogen to form alkanes.
* Alkenes can be used to produce addition polymers, which are used to make plastics.
* Alkenes have lower boiling points than alkanes, but the boiling point increases as the size of the molecule increase
how do you name alkenes
*Find the longest carbon chain that contains the double bond
* Name like an alkane but use - ene. Use “-diene” for two, or “-triene” for three double bonds.
* Number the carbons so the double bond carbons have the lowest possible numbers.
* State the number before the -ene with a dash, e.g. hex-1-ene
Remember to name side chains and the double bond as low as possible
what are the 2 types of stereoisomerism?
- E-Z isomers: caused by molecules with a C=C with two different groups attached to each C of the C=C
- optical isomers: caused by C with atoms having four different groups attached leading to molecules that are non superimposable mirror images of each other